Quality Control Analyst - Pharmaceuticals

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Irfa******

  • United States 
  • Last Update: 18.10.2019 at 12:00

Job Type
Full Time
Start
ASAP
Duration
3 Month +
Place
Le Sueur, MN, US
Country
United States

Description


If you are a Quality Control Analyst with experience, please read on!

We are an international developer, manufacturer and marketer of veterinary pharmaceuticals and animal health products. In addition to distributing our branded products in over seventy countries world-wide, we also manufacture private label for distributors, agents and international companies.

We are looking for an experienced QC Analyst to join our dynamic and committed team in Le Sueur, MN. Join us!

What You Will Be Doing
  • Receive and log into the laboratory all samples required for analytical support.
  • Perform all quality control analytical methods as required to support Production.
  • Assist in the transfer of USP methods for all new products that are developed in-house and/or site transferred into the facility.
  • Perform review of notebooks and raw data for samples analyzed in the laboratory.
  • Perform out-of-specification investigations and all required documentation per cGMPs and company procedures.
  • Support Continuous Improvement program throughout the company.
  • Operate, troubleshoot, and maintain analytical equipment used in the laboratory, such as HPLC, GC, FTIR, dissolution apparatus, and TOC analyzer.
  • Interface with FDA compliance officers during facility inspections.
  • Review and revise procedures as required to ensure compliance.
  • Review and revise analytical methods.
  • Accurately document all data in compliance with GMP.
  • Perform QA lines check as needed during filling and labelling to support Production.
  • Perform method verification and validation for HPLC, GC, and other tests.
What You Need for this Position
  • 1-5 years of analytical chemistry experience
  • Practical experience with GMPs within a regulated environment
  • Bachelors Degree in related science field.
  • Working knowledge and troubleshooting of HPLC and GC
  • (preferred) Experience in an FDA, Canadian Health, and or EU regulated Pharmaceutical manufacturing environment
  • (preferred) Knowledge of USP methodologies
  • (preferred) Knowledge and troubleshooting of FTIR, UV/VIS, and dissolution apparatus.
What's In It for You
  • $40,000 - $65,000 (depending on experience)
  • PTO
  • Medical/Dental/Vision/Life/Disability
  • 401K Matching
  • Pension Plan
  • Performance Bonus
So, if you are a Quality Control Analyst with experience, please apply today!

Email Your Resume In Word To

Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, but you may also:

Sarah.Ellis@CyberCoders.com
  • Please do NOT change the email subject line in any way. You must keep the JobID: linkedin : SE5-1552447 -- in the email subject line for your application to be considered.***
Sarah Ellis - Executive Recruiter - CyberCoders

Applicants must be authorized to work in the U.S.

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